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Items: 1 to 20 of 135

1.

Variants at the 9p21 locus and melanoma risk.

Maccioni L, Rachakonda PS, Bermejo JL, Planelles D, Requena C, Hemminki K, Nagore E, Kumar R.

BMC Cancer. 2013 Jul 2;13:325. doi: 10.1186/1471-2407-13-325.

2.

Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations.

Yang XR, Liang X, Pfeiffer RM, Wheeler W, Maeder D, Burdette L, Yeager M, Chanock S, Tucker MA, Goldstein AM.

Fam Cancer. 2010 Dec;9(4):625-33. doi: 10.1007/s10689-010-9356-3.

3.

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.

Falchi M, Bataille V, Hayward NK, Duffy DL, Bishop JA, Pastinen T, Cervino A, Zhao ZZ, Deloukas P, Soranzo N, Elder DE, Barrett JH, Martin NG, Bishop DT, Montgomery GW, Spector TD.

Nat Genet. 2009 Aug;41(8):915-9. doi: 10.1038/ng.410.

4.

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.

Chen SN, Ballantyne CM, Gotto AM Jr, Marian AJ.

BMC Cardiovasc Disord. 2009 Jan 27;9:3. doi: 10.1186/1471-2261-9-3.

5.

A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.

Osman W, Low SK, Takahashi A, Kubo M, Nakamura Y.

Hum Mol Genet. 2012 Jun 15;21(12):2836-42. doi: 10.1093/hmg/dds103.

6.

Variants at chromosome 20 (ASIP locus) and melanoma risk.

Maccioni L, Rachakonda PS, Scherer D, Bermejo JL, Planelles D, Requena C, Hemminki K, Nagore E, Kumar R.

Int J Cancer. 2013 Jan 1;132(1):42-54. doi: 10.1002/ijc.27648.

7.

Genetic analysis of three important genes in pigmentation and melanoma susceptibility: CDKN2A, MC1R and HERC2/OCA2.

Ibarrola-Villava M, Fernandez LP, Pita G, Bravo J, Floristan U, Sendagorta E, Feito M, Avilés JA, Martin-Gonzalez M, Lázaro P, Benítez J, Ribas G.

Exp Dermatol. 2010 Sep;19(9):836-44. doi: 10.1111/j.1600-0625.2010.01115.x.

PMID:
20629734
8.

Contribution of melanocortin-1 receptor gene variants to sporadic cutaneous melanoma risk in a population in central Italy: a case-control study.

Fargnoli MC, Altobelli E, Keller G, Chimenti S, Höfler H, Peris K.

Melanoma Res. 2006 Apr;16(2):175-82.

PMID:
16567973
9.

The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.

Cheng X, Shi L, Nie S, Wang F, Li X, Xu C, Wang P, Yang B, Li Q, Pan Z, Li Y, Xia H, Zheng C, Ke Y, Wu Y, Tang T, Yan X, Yang Y, Xia N, Yao R, Wang B, Ma X, Zeng Q, Tu X, Liao Y, Wang QK.

Diabetes. 2011 Feb;60(2):680-4. doi: 10.2337/db10-0185.

10.

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.

Smith JG, Melander O, Lövkvist H, Hedblad B, Engström G, Nilsson P, Carlson J, Berglund G, Norrving B, Lindgren A.

Circ Cardiovasc Genet. 2009 Apr;2(2):159-64. doi: 10.1161/CIRCGENETICS.108.835173.

11.

Genetic variants in loci 1p13 and 9p21 and fatal coronary heart disease in a Norwegian case-cohort study.

Jansen MD, Knudsen GP, Myhre R, Høiseth G, Mørland J, Næss Ø, Tambs K, Magnus P.

Mol Biol Rep. 2014 May;41(5):2733-43. doi: 10.1007/s11033-014-3096-7.

PMID:
24728607
12.

MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis.

Fargnoli MC, Gandini S, Peris K, Maisonneuve P, Raimondi S.

Eur J Cancer. 2010 May;46(8):1413-20. doi: 10.1016/j.ejca.2010.01.027. Review.

PMID:
20189796
13.

Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control study.

Stefanaki I, Panagiotou OA, Kodela E, Gogas H, Kypreou KP, Chatzinasiou F, Nikolaou V, Plaka M, Kalfa I, Antoniou C, Ioannidis JP, Evangelou E, Stratigos AJ.

PLoS One. 2013;8(2):e55712. doi: 10.1371/journal.pone.0055712.

14.

MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population.

Landi MT, Kanetsky PA, Tsang S, Gold B, Munroe D, Rebbeck T, Swoyer J, Ter-Minassian M, Hedayati M, Grossman L, Goldstein AM, Calista D, Pfeiffer RM.

J Natl Cancer Inst. 2005 Jul 6;97(13):998-1007. Erratum in: J Natl Cancer Inst. 2005 Sep 21;97(18):1385.

15.

A genome-wide association study of a coronary artery disease risk variant.

Lee JY, Lee BS, Shin DJ, Woo Park K, Shin YA, Joong Kim K, Heo L, Young Lee J, Kyoung Kim Y, Jin Kim Y, Bum Hong C, Lee SH, Yoon D, Jung Ku H, Oh IY, Kim BJ, Lee J, Park SJ, Kim J, Kawk HK, Lee JE, Park HK, Lee JE, Nam HY, Park HY, Shin C, Yokota M, Asano H, Nakatochi M, Matsubara T, Kitajima H, Yamamoto K, Kim HL, Han BG, Cho MC, Jang Y, Kim HS, Euy Park J, Lee JY.

J Hum Genet. 2013 Mar;58(3):120-6. doi: 10.1038/jhg.2012.124.

PMID:
23364394
16.

Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.

Çakmak HA, Bayoğlu B, Durmaz E, Can G, Karadağ B, Cengiz M, Vural VA, Yüksel H.

Anatol J Cardiol. 2015 Mar;15(3):196-203. doi: 10.5152/akd.2014.5285.

17.
18.

Genome-wide association study identifies three loci associated with melanoma risk.

Bishop DT, Demenais F, Iles MM, Harland M, Taylor JC, Corda E, Randerson-Moor J, Aitken JF, Avril MF, Azizi E, Bakker B, Bianchi-Scarrà G, Bressac-de Paillerets B, Calista D, Cannon-Albright LA, Chin-A-Woeng T, Debniak T, Galore-Haskel G, Ghiorzo P, Gut I, Hansson J, Hocevar M, Höiom V, Hopper JL, Ingvar C, Kanetsky PA, Kefford RF, Landi MT, Lang J, Lubiński J, Mackie R, Malvehy J, Mann GJ, Martin NG, Montgomery GW, van Nieuwpoort FA, Novakovic S, Olsson H, Puig S, Weiss M, van Workum W, Zelenika D, Brown KM, Goldstein AM, Gillanders EM, Boland A, Galan P, Elder DE, Gruis NA, Hayward NK, Lathrop GM, Barrett JH, Bishop JA.

Nat Genet. 2009 Aug;41(8):920-5. doi: 10.1038/ng.411.

19.

Melanoma risk associated with MC1R gene variants in Latvia and the functional analysis of rare variants.

Ozola A, Azarjana K, Doniņa S, Proboka G, Mandrika I, Petrovska R, Cēma I, Heisele O, Eņģele L, Streinerte B, Pjanova D.

Cancer Genet. 2013 Mar;206(3):81-91. doi: 10.1016/j.cancergen.2013.01.002.

PMID:
23522749
20.

Influence of genetic variants in type I interferon genes on melanoma survival and therapy.

Lenci RE, Bevier M, Brandt A, Bermejo JL, Sucker A, Moll I, Planelles D, Requena C, Nagore E, Hemminki K, Schadendorf D, Kumar R.

PLoS One. 2012;7(11):e50692. doi: 10.1371/journal.pone.0050692.

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